Author:
Mendelsohn F. A. O.,Kachel Christine D.
Abstract
Abstract.
Normal human serum markedly stimulated aldosterone production from rat adrenal glomerulosa cells incubated in Krebs Ringer bicarbonate medium (KRBGA). The effect was dose-related. In [K+] 3.6 mm KRBGA medium, serum stimulated aldosterone output to higher levels than those produced by maximal doses of serotonin (5 HT), angiotensin II (AII) or high [K+] (8.4 mm).
Cells maximally stimulated by high [K+], 5 HT or AII in KRBGA medium were further stimulated by serum. The angiotensin analogue, [Sar1, Ala8]-AII abolished the effect of AII but not that of high [K+] or serum.
Basal and ACTH-stimulated corticosterone outputs of rat fasciculata cells were not significantly affected by sera known to stimulate glomerulosa cells.
Aldosterone stimulating activity of serum was dialysable and fully recovered in a serum ultrafiltrate.
The serotonin blockers methysergide and metergoline abolished the aldosterone stimulating activity of serum but also depressed basal aldosterone output and methysergide reduced K+-stimulated output.
Chymotrypsin digestion abolished the aldosterone stimulating activity of AII but not that of serotonin or serum.
5 HT concentration of sera was measured and found to be near the threshold for aldosterone stimulation.
Sodium loading and depletion of 4 normal subjects did not consistently modify the aldosterone stimulating activity of their sera.
In a supplemented medium (RPMI 1640), basal and K+-stimulated aldosterone outputs were higher than in KRBGA medium. Under these conditions serum stimulated aldosterone output in normal [K+] medium but only marginally in high [K+] medium. In RPMI medium, serum did not further stimulate cells maximally stimulated with serotonin.
Serum appears to stimulate aldosterone production from glomerulsoa cells by two different mechanisms: One is probably due to a serotonin-like substance. A separate effect of serum, seen only in KRBGA medium, is to enhance aldosterone output of glomerulosa cells maximally stimulated by K+, 5 HT or AII.
Subject
Endocrinology,General Medicine,Endocrinology, Diabetes and Metabolism
Cited by
6 articles.
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